Biomimetic Magnetosomes as Versatile Artificial Antigen-Presenting Cells to Potentiate T-Cell-Based Anticancer Therapy

被引:168
|
作者
Zhang, Qanmei [1 ]
Wei, Wei [2 ]
Wang, Peilin [1 ]
Zuo, Liping [1 ]
Li, Feng [1 ]
Xu, Jin [1 ]
Xi, Xiaobo [2 ]
Gao, Xiaoyong [2 ]
Ma, Guanghui [2 ]
Xie, Hai-Yan [1 ]
机构
[1] Beijing Inst Technol, Sch Life Sci, Beijing 100081, Peoples R China
[2] Chinese Acad Sci, Inst Proc Engn, Natl Key Lab Biochem Engn, Beijing 100190, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
biomimetic; artificial antigen-presenting cells; targeting delivery; T-cell therapy; CANCER-IMMUNOTHERAPY; BIOLOGICAL BARRIERS; DRUG-DELIVERY; TUMOR-CELLS; NANOPARTICLES; ACTIVATION; LYMPHOCYTES; MEMBRANE;
D O I
10.1021/acsnano.7b04955
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Adoptive T-cell transfer for cancer therapy relies on both effective ex vivo T-cell expansion and in vivo targeting performance. One promising but challenging method for accomplishing this purpose is to construct multifunctional artificial antigen-presenting cells (aAPCs). We herein developed biomimetic magnetosomes as versatile aAPCs, wherein magnetic nanoclusters were coated with azide-engineered leucocyte membranes and then decorated with T-cell stimuli through copper-free click chemistry. These nano aAPCs not only exhibited high performance for antigen-specific cytotoxic T-cell (CTL) expansion and stimulation but also visually and effectively guided reinfused CTLs to tumor tissues through magnetic resonance imaging and magnetic control. The persisting T cells were able to delay tumor growth in a murine lymphoma model, while the systemic toxicity was not notable. These results together demonstrated the excellent potential of this "one-but-all" aAPC platform for T-cell-based anticancer immunotherapy.
引用
收藏
页码:10724 / 10732
页数:9
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